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(R)-1-chlorohex-5-en-2-ol, with the molecular formula C6H11ClO, is a chiral chemical compound characterized by its non-superimposable mirror image. As a colorless liquid, it features both a chloroalkene group and an alcohol group, classifying it as an alkene and an alcohol. Its unique chiral nature renders it valuable in various applications, particularly in the synthesis of pharmaceuticals, agrochemicals, and for research in stereoisomerism and enantioselective synthesis.

1374009-33-2

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1374009-33-2 Usage

Uses

Used in Organic Synthesis:
(R)-1-chlorohex-5-en-2-ol is utilized as a key building block in organic synthesis, contributing to the creation of a diverse range of chemical compounds. Its presence in this application is attributed to its versatile molecular structure, which allows for further functionalization and the development of novel molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (R)-1-chlorohex-5-en-2-ol is employed as an intermediate in the synthesis of various drugs. Its chiral nature is particularly advantageous, as it enables the production of enantiomerically pure compounds, which are essential for ensuring the desired therapeutic effects and minimizing potential side effects.
Used in Agrochemical Production:
(R)-1-chlorohex-5-en-2-ol also finds application in the agrochemical sector, where it serves as a starting material for the synthesis of biologically active compounds. These compounds are often used in the development of pesticides, herbicides, and other agricultural products, highlighting the compound's importance in supporting the agricultural industry.
Used in Stereoisomerism and Enantioselective Synthesis Research:
The chiral nature of (R)-1-chlorohex-5-en-2-ol makes it an ideal candidate for research in stereoisomerism and enantioselective synthesis. In this context, it is used to study the effects of stereochemistry on the properties and reactivity of molecules, as well as to develop new methods for the selective synthesis of enantiomers, which is crucial for the advancement of the chemical sciences and the development of more effective drugs and chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 1374009-33-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,0,0 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1374009-33:
(9*1)+(8*3)+(7*7)+(6*4)+(5*0)+(4*0)+(3*9)+(2*3)+(1*3)=142
142 % 10 = 2
So 1374009-33-2 is a valid CAS Registry Number.

1374009-33-2Upstream product

1374009-33-2Downstream Products

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